Organic molybdenum compounds and lubricating compositions which contain said compounds

ABSTRACT

Dicyclopentadienyl molybdenum crosslinked complexes which can be represented by general formula (1) below are provided, the use thereof as friction-modifiers and lubricating compositions which contain these compounds are also provided 
                         
In this formula X is the element oxygen or the element sulphur, Y is the element oxygen or Y is absent, and R 1  to R 10  are groups selected individually from the group comprising hydrogen, the methyl group and the ethyl group.

CROSS-REFERENCE TO RELATED APPLICATIONS

The present application is a continuation of U.S. Ser. No. 12/525,359,filed on Nov. 25, 2009, which claims priority from PCT/US2008/051258,filed Feb. 1, 2008, which claims priority from JP 2007-023479, filedFeb. 1, 2007, all of which are incorporated herein by reference.

TECHNICAL FIELD OF THE INVENTION

The invention relates to novel organic molybdenum compounds, the usethereof as friction-modifiers and lubricating compositions which containsaid compounds.

BACKGROUND OF THE INVENTION

Friction-modifiers (friction-adjusting agents) are used for adjustingthe friction characteristics of a lubricant to an appropriate level.Friction-modifiers which reduce friction are used in lubricatingcompositions such as gear oils and engine oils with a view to reducingfuel costs. Friction-modifiers which raise friction are used formaintaining a certain high friction level in the lubricatingcompositions which are used in the wet-type clutch part of an automaticgear box. Many types of such friction-modifiers have been proposed.

The organic molybdenum compounds are the most typical of thesefriction-modifiers and, as shown in “Shinban Sekiyu Seihin Tenkasai”(New Edition, Additives for Petroleum Products), by Toshio SAKURAI,Saiwai Shobo Co., published 25 Jul. 1986, these organic molybdenumcompounds are compounds which have two molybdenum atoms in one moleculeas shown in formulae (2) and (3) below.

(Those compounds for which in this formulae x=0 and y=4, and for whichx+y=4, and for which x≧2 are insoluble in oil and the others areoil-soluble.)

Furthermore, compounds in which the element molybdenum is included twicein one molecule have been disclosed in Japanese Patent No. 3495764,Japanese Examined Patent Publication 45-24562, Japanese UnexaminedPatent Application Laid Open 52-19629, Japanese Unexamined PatentApplication Laid Open 52-106824, and Japanese Unexamined PatentApplication Laid Open 48-56202.

A problem with catalyst poisoning in the apparatus which is used forcleaning-up the exhaust gas arises when compounds which containphosphorus in the molecule as shown in the aforementioned generalformula (2) are added to engine oils and there is a demand for compoundswhich are phosphorus-free.

SUMMARY OF THE INVENTION

An object of the present invention is to provide novel compounds whichare useful as lubricating additives and the like which do not containphosphorus, which reduce the friction coefficient and control thefriction of a wet-type clutch, for example, optimally, and frictionmodifiers comprising said compounds.

A further object of the invention is to provide lubricating compositionswhich contain these compounds.

BRIEF EXPLANATION OF THE DRAWINGS

FIG. 1 is a graph showing how the friction coefficient changed with thepassage of time with the lubricating oils of Example 5 and ComparativeExample 1.

FIG. 2 is an outline drawing of the cylinder-on-disc reciprocatingmovement tester.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

To achieve these objects, the present invention providesdicyclopentadienyl molybdenum crosslinked complexes having generalformula (1) below.

In this formula X is the element oxygen or the element sulphur, Y is theelement oxygen or Y is absent, and R¹ to R¹⁰ are groups selectedindividually from the group comprising hydrogen, a methyl group and anethyl group.

According to a preferred embodiment the dicyclopentadienyl molybdenumcrosslinked complexes of general formula (1) can be represented bygeneral formula (2) which is indicated below.

In this formula R¹ to R¹⁰ are groups selected individually from thegroup comprising hydrogen, a methyl group and an ethyl group.

According to a preferred embodiment the dicyclopentadienyl molybdenumcrosslinked complexes of general formula (1) can be represented bygeneral formula (3) which is indicated below.

In this formula R¹ to R¹⁰ are groups selected individually from thegroup comprising hydrogen, a methyl group and an ethyl group.

According to a preferred embodiment the dicyclopentadienyl molybdenumcrosslinked complexes of general formula (1) can be represented bygeneral formula (4) which is indicated below.

In this

formula R¹ to R¹⁰ are groups selected individually from the groupcomprising hydrogen, a methyl group and an ethyl group.

According to a preferred embodiment the dicyclopentadienyl molybdenumcrosslinked complexes of general formula (1) can be represented bygeneral formula (5) which is indicated below.

In this formula R¹ to R¹⁰ are groups selected individually from thegroup comprising hydrogen, a methyl group and an ethyl group.

Further the present invention provides the use of the dicyclopentadienylmolybdenum crosslinked complexes as friction-modifiers.

Also the present invention provides lubricating compositions whichcontain the compounds.

The compounds of this invention can be produced, for example, using themethod indicated below.

First Process

Synthesis of the Synthesis Intermediate Raw Material DicyclopentadienylMolybdenum Hexa-Carbonyl Complex

Second Process

Synthesis of the Dicyclopentadienyl Molybdenum Crosslinked Complex

The di(cyclopentadienyl) μ-thioxomolybdenum complex of general formula(2), the di(cyclopentadienyl) μ-thioxodioxomolybdenum complex of generalformula (3), the di(cyclopentadienyl) μ-oxomolybdenum complex of generalformula (4) and the di(cyclopentadienyl) μ-oxodioxomolybdenum complex ofgeneral formula (5) are produced simultaneously in accordance with thereaction equation indicated below.

Hydrogen, the methyl group and the ethyl group can be cited for theaforementioned R¹ to R¹⁰, and the compounds with combinations such asthose shown in Tables 1 to 18 below can be cited.

TABLE 1 Compound 1 2 3 4 5 6 7 8 X S S O O S S O O Y O — O — O — O — R¹H H H H CH₃ CH₃ CH₃ CH₃ R² H H H H CH₃ CH₃ CH₃ CH₃ R³ H H H H CH₃ CH₃CH₃ CH₃ R⁴ H H H H CH₃ CH₃ CH₃ CH₃ R⁵ H H H H CH₃ CH₃ CH₃ CH₃ R⁶ H H H HCH₃ CH₃ CH₃ CH₃ R⁷ H H H H CH₃ CH₃ CH₃ CH₃ R⁸ H H H H CH₃ CH₃ CH₃ CH₃ R⁹H H H H CH₃ CH₃ CH₃ CH₃ R¹⁰ H H H H CH₃ CH₃ CH₃ CH₃

TABLE 2 Compound 9 10 11 12 13 14 15 16 X S S O O S S O O Y O — O — O —O — R¹ C₂H₅ C₂H₅ C₂H₅ C₂H₅ H H H H R² C₂H₅ C₂H₅ C₂H₅ C₂H₅ H H H H R³C₂H₅ C₂H₅ C₂H₅ C₂H₅ H H H H R⁴ C₂H₅ C₂H₅ C₂H₅ C₂H₅ H H H H R⁵ C₂H₅ C₂H₅C₂H₅ C₂H₅ H H H H R⁶ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ R⁷ C₂H₅C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ R⁸ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅C₂H₅ R⁹ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ R¹⁰ C₂H₅ C₂H₅ C₂H₅ C₂H₅C₂H₅ C₂H₅ C₂H₅ C₂H₅

TABLE 3 Compound 17 18 19 20 21 22 23 24 X S S O O S S O O Y O — O — O —O — R¹ H H H H CH₃ CH₃ CH₃ CH₃ R² H H H H H H H H R³ H H H H H H H H R⁴H H H H H H H H R⁵ H H H H H H H H R⁶ CH₃ CH₃ CH₃ CH₃ CH₃ CH₃ CH₃ CH₃ R⁷CH₃ CH₃ CH₃ CH₃ H H H H R⁸ CH₃ CH₃ CH₃ CH₃ H H H H R⁹ CH₃ CH₃ CH₃ CH₃ HH H H R¹⁰ CH₃ CH₃ CH₃ CH₃ H H H H

TABLE 4 Compound 25 26 27 28 29 30 31 32 X S S O O S S O O Y O — O — O —O — R¹ CH₃ CH₃ CH₃ CH₃ CH₃ CH₃ CH₃ CH₃ R² CH₃ CH₃ CH₃ CH₃ H H H H R³ H HH H CH₃ CH₃ CH₃ CH₃ R⁴ H H H H H H H H R⁵ H H H H H H H H R⁶ CH₃ CH₃ CH₃CH₃ CH₃ CH₃ CH₃ CH₃ R⁷ CH₃ CH₃ CH₃ CH₃ H H H H R⁸ H H H H CH₃ CH₃ CH₃CH₃ R⁹ H H H H H H H H R¹⁰ H H H H H H H H

TABLE 5 Compound 33 34 35 36 37 38 39 40 X S S O O S S O O Y O — O — O —O — R¹ CH₃ CH₃ CH₃ CH₃ CH₃ CH₃ CH₃ CH₃ R² CH₃ CH₃ CH₃ CH₃ CH₃ CH₃ CH₃CH₃ R³ CH₃ CH₃ CH₃ CH₃ H H H H R⁴ H H H H CH₃ CH₃ CH₃ CH₃ R⁵ H H H H H HH H R⁶ CH₃ CH₃ CH₃ CH₃ CH₃ CH₃ CH₃ CH₃ R⁷ CH₃ CH₃ CH₃ CH₃ CH₃ CH₃ CH₃CH₃ R⁸ CH₃ CH₃ CH₃ CH₃ H H H H R⁹ H H H H CH₃ CH₃ CH₃ CH₃ R¹⁰ H H H H HH H H

TABLE 6 Compound 41 42 43 44 45 46 47 48 X S S O O S S O O Y O — O — O —O — R¹ CH₃ CH₃ CH₃ CH₃ C₂H₅ C₂H₅ C₂H₅ C₂H₅ R² CH₃ CH₃ CH₃ CH₃ H H H H R³CH₃ CH₃ CH₃ CH₃ H H H H R⁴ CH₃ CH₃ CH₃ CH₃ H H H H R⁵ H H H H H H H H R⁶CH₃ CH₃ CH₃ CH₃ C₂H₅ C₂H₅ C₂H₅ C₂H₅ R⁷ CH₃ CH₃ CH₃ CH₃ H H H H R⁸ CH₃CH₃ CH₃ CH₃ H H H H R⁹ CH₃ CH₃ CH₃ CH₃ H H H H R¹⁰ H H H H H H H H

TABLE 7 Compound 49 50 51 52 53 54 55 56 X S S O O S S O O Y O — O — O —O — R¹ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ R² C₂H₅ C₂H₅ C₂H₅ C₂H₅ HH H H R³ H H H H C₂H₅ C₂H₅ C₂H₅ C₂H₅ R⁴ H H H H H H H H R⁵ H H H H H H HH R⁶ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ R⁷ C₂H₅ C₂H₅ C₂H₅ C₂H₅ H HH H R⁸ H H H H C₂H₅ C₂H₅ C₂H₅ C₂H₅ R⁹ H H H H H H H H R¹⁰ H H H H H H HH

TABLE 8 Compound 57 58 59 60 61 62 63 64 X S S O O S S O O Y O — O — O —O — R¹ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ R² C₂H₅ C₂H₅ C₂H₅ C₂H₅C₂H₅ C₂H₅ C₂H₅ C₂H₅ R³ C₂H₅ C₂H₅ C₂H₅ C₂H₅ H H H H R⁴ H H H H C₂H₅ C₂H₅C₂H₅ C₂H₅ R⁵ H H H H H H H H R⁶ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅R⁷ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ R⁸ C₂H₅ C₂H₅ C₂H₅ C₂H₅ H H HH R⁹ H H H H C₂H₅ C₂H₅ C₂H₅ C₂H₅ R¹⁰ H H H H H H H H

TABLE 9 Compound 65 66 67 68 69 70 71 72 X S S O O S S O O Y O — O — O —O — R¹ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ R² C₂H₅ C₂H₅ C₂H₅ C₂H₅CH₃ CH₃ CH₃ CH₃ R³ C₂H₅ C₂H₅ C₂H₅ C₂H₅ CH₃ CH₃ CH₃ CH₃ R⁴ C₂H₅ C₂H₅ C₂H₅C₂H₅ CH₃ CH₃ CH₃ CH₃ R⁵ H H H H CH₃ CH₃ CH₃ CH₃ R⁶ C₂H₅ C₂H₅ C₂H₅ C₂H₅C₂H₅ C₂H₅ C₂H₅ C₂H₅ R⁷ C₂H₅ C₂H₅ C₂H₅ C₂H₅ CH₃ CH₃ CH₃ CH₃ R⁸ C₂H₅ C₂H₅C₂H₅ C₂H₅ CH₃ CH₃ CH₃ CH₃ R⁹ C₂H₅ C₂H₅ C₂H₅ C₂H₅ CH₃ CH₃ CH₃ CH₃ R¹⁰ H HH H CH₃ CH₃ CH₃ CH₃

TABLE 10 Compound 73 74 75 76 77 78 79 80 X S S O O S S O O Y O — O — O— O — R¹ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ R² C₂H₅ C₂H₅ C₂H₅ C₂H₅CH₃ CH₃ CH₃ CH₃ R³ CH₃ CH₃ CH₃ CH₃ C₂H₅ C₂H₅ C₂H₅ C₂H₅ R⁴ CH₃ CH₃ CH₃CH₃ CH₃ CH₃ CH₃ CH₃ R⁵ CH₃ CH₃ CH₃ CH₃ CH₃ CH₃ CH₃ CH₃ R⁶ C₂H₅ C₂H₅ C₂H₅C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ R⁷ C₂H₅ C₂H₅ C₂H₅ C₂H₅ CH₃ CH₃ CH₃ CH₃ R⁸ CH₃CH₃ CH₃ CH₃ C₂H₅ C₂H₅ C₂H₅ C₂H₅ R⁹ CH₃ CH₃ CH₃ CH₃ CH₃ CH₃ CH₃ CH₃ R¹⁰CH₃ CH₃ CH₃ CH₃ CH₃ CH₃ CH₃ CH₃

TABLE 11 Compound 81 82 83 84 85 86 87 88 X S S O O S S O O Y O — O — O— O — R¹ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ R² C₂H₅ C₂H₅ C₂H₅ C₂H₅C₂H₅ C₂H₅ C₂H₅ C₂H₅ R³ C₂H₅ C₂H₅ C₂H₅ C₂H₅ CH₃ CH₃ CH₃ CH₃ R⁴ CH₃ CH₃CH₃ CH₃ C₂H₅ C₂H₅ C₂H₅ C₂H₅ R⁵ CH₃ CH₃ CH₃ CH₃ CH₃ CH₃ CH₃ CH₃ R⁶ C₂H₅C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ R⁷ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅C₂H₅ R⁸ C₂H₅ C₂H₅ C₂H₅ C₂H₅ CH₃ CH₃ CH₃ CH₃ R⁹ CH₃ CH₃ CH₃ CH₃ C₂H₅ C₂H₅C₂H₅ C₂H₅ R¹⁰ CH₃ CH₃ CH₃ CH₃ CH₃ CH₃ CH₃ CH₃

TABLE 12 Compound 89 90 91 92 93 94 95 96 X S S O O S S O O Y O — O — O— O — R¹ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ R² C₂H₅ C₂H₅ C₂H₅ C₂H₅CH₃ CH₃ CH₃ CH₃ R³ C₂H₅ C₂H₅ C₂H₅ C₂H₅ H H H H R⁴ C₂H₅ C₂H₅ C₂H₅ C₂H₅ HH H H R⁵ CH₃ CH₃ CH₃ CH₃ H H H H R⁶ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅C₂H₅ R⁷ C₂H₅ C₂H₅ C₂H₅ C₂H₅ CH₃ CH₃ CH₃ CH₃ R⁸ C₂H₅ C₂H₅ C₂H₅ C₂H₅ H H HH R⁹ C₂H₅ C₂H₅ C₂H₅ C₂H₅ H H H H R¹⁰ CH₃ CH₃ CH₃ CH₃ H H H H

TABLE 13 Compound 97 98 99 100 101 102 103 104 X S S O O S S O O Y O — O— O — O — R¹ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ R² H H H H CH₃ CH₃CH₃ CH₃ R³ CH₃ CH₃ CH₃ CH₃ CH₃ CH₃ CH₃ CH₃ R⁴ H H H H H H H H R⁵ H H H HH H H H R⁶ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ R⁷ H H H H CH₃ CH₃CH₃ CH₃ R⁸ CH₃ CH₃ CH₃ CH₃ CH₃ CH₃ CH₃ CH₃ R⁹ H H H H H H H H R¹⁰ H H HH H H H H

TABLE 14 Compound 105 106 107 108 109 110 111 112 X S S O O S S O O Y O— O — O — O — R¹ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ R² CH₃ CH₃ CH₃CH₃ CH₃ CH₃ CH₃ CH₃ R³ CH₃ CH₃ CH₃ CH₃ CH₃ CH₃ CH₃ CH₃ R⁴ CH₃ CH₃ CH₃CH₃ H H H H R⁵ H H H H CH₃ CH₃ CH₃ CH₃ R⁶ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅C₂H₅ C₂H₅ R⁷ CH₃ CH₃ CH₃ CH₃ CH₃ CH₃ CH₃ CH₃ R⁸ CH₃ CH₃ CH₃ CH₃ CH₃ CH₃CH₃ CH₃ R⁹ CH₃ CH₃ CH₃ CH₃ H H H H R¹⁰ H H H H CH₃ CH₃ CH₃ CH₃

TABLE 15 Compound 113 114 115 116 117 118 119 120 X S S O O S S O O Y O— O — O — O — R¹ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ R² C₂H₅ C₂H₅C₂H₅ C₂H₅ CH₃ CH₃ CH₃ CH₃ R³ CH₃ CH₃ CH₃ CH₃ C₂H₅ C₂H₅ C₂H₅ C₂H₅ R⁴ H HH H H H H H R⁵ H H H H H H H H R⁶ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅C₂H₅ R⁷ C₂H₅ C₂H₅ C₂H₅ C₂H₅ CH₃ CH₃ CH₃ CH₃ R⁸ CH₃ CH₃ CH₃ CH₃ C₂H₅ C₂H₅C₂H₅ C₂H₅ R⁹ H H H H H H H H R¹⁰ H H H H H H H H

TABLE 16 Compound 121 122 123 124 125 126 127 128 X S S O O S S O O Y O— O — O — O — R¹ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ R² H H H H C₂H₅C₂H₅ C₂H₅ C₂H₅ R³ C₂H₅ C₂H₅ C₂H₅ C₂H₅ CH₃ CH₃ CH₃ CH₃ R⁴ H H H H CH₃ CH₃CH₃ CH₃ R⁵ CH₃ CH₃ CH₃ CH₃ H H H H R⁶ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅C₂H₅ R⁷ H H H H C₂H₅ C₂H₅ C₂H₅ C₂H₅ R⁸ C₂H₅ C₂H₅ C₂H₅ C₂H₅ CH₃ CH₃ CH₃CH₃ R⁹ H H H H CH₃ CH₃ CH₃ CH₃ R¹⁰ CH₃ CH₃ CH₃ CH₃ H H H H

TABLE 17 Compound 129 130 131 132 133 134 135 136 X S S O O S S O O Y O— O — O — O — R¹ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ R² CH₃ CH₃ CH₃CH₃ H H H H R³ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ R⁴ CH₃ CH₃ CH₃CH₃ CH₃ CH₃ CH₃ CH₃ R⁵ H H H H CH₃ CH₃ CH₃ CH₃ R⁶ C₂H₅ C₂H₅ C₂H₅ C₂H₅C₂H₅ C₂H₅ C₂H₅ C₂H₅ R⁷ CH₃ CH₃ CH₃ CH₃ H H H H R⁸ C₂H₅ C₂H₅ C₂H₅ C₂H₅C₂H₅ C₂H₅ C₂H₅ C₂H₅ R⁹ CH₃ CH₃ CH₃ CH₃ CH₃ CH₃ CH₃ CH₃ R¹⁰ H H H H CH₃CH₃ CH₃ CH₃

TABLE 18 Compound 137 138 139 140 141 142 143 144 X S S O O S S O O Y O— O — O — O — R¹ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ R² C₂H₅ C₂H₅C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ R³ C₂H₅ C₂H₅ C₂H₅ C₂H₅ CH₃ CH₃ CH₃ CH₃ R⁴CH₃ CH₃ CH₃ CH₃ C₂H₅ C₂H₅ C₂H₅ C₂H₅ R⁵ H H H H H H H H R⁶ C₂H₅ C₂H₅ C₂H₅C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ R⁷ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ C₂H₅ R⁸C₂H₅ C₂H₅ C₂H₅ C₂H₅ CH₃ CH₃ CH₃ CH₃ R⁹ CH₃ CH₃ CH₃ CH₃ C₂H₅ C₂H₅ C₂H₅C₂H₅ R¹⁰ H H H H H H H H

Lubricating oils and greases, for example, can be cited as lubricatingcompositions of this invention. The amount of a compound of thisinvention in a lubricating composition is the same as with theconventional friction-modifiers, for example, being compounded in aproportion with respect to the composition generally of some 0.1 to 10wt %.

There are no particular limitations regarding the base oil or greaseused in lubricating composition according to the present invention, andvarious conventional greases, mineral oils and synthetic oils may beconveniently used. For the purpose of this description, the term “baseoil” is meant to also include a grease base stock.

The base oil used in the present invention may conveniently comprisemixtures of one or more mineral oils and/or one or more synthetic oils.

Mineral oils include liquid petroleum oils and solvent-treated oracid-treated mineral lubricating oil of the paraffinic, naphthenic, ormixed paraffinic/naphthenic type which may be further refined byhydrofinishing processes and/or dewaxing.

Suitable base oils for use in the lubricating oil composition of thepresent invention are Group I, Group II or Group III base oils,polyalphaolefins, Fischer-Tropsch derived base oils and mixturesthereof.

By “Group I” base oil, “Group II” base oil and “Group III” base oil inthe present invention are meant lubricating oil base oils according tothe definitions of American Petroleum Institute (API) categories I, IIand III. Such API categories are defined in API Publication 1509, 15thEdition, Appendix E, April 2002.

Suitable Fischer-Tropsch derived base oils that may be conveniently usedas the base oil in the lubricating oil composition of the presentinvention are those as for example disclosed in EP 0 776 959, EP 0 668342, WO 97/21788, WO 00/15736, WO 00/14188, WO 00/14187, WO 00/14183, WO00/14179, WO 00/08115, WO 99/41332, EP 1 029 029, WO 01/18156 and WO01/57166.

Synthetic oils include hydrocarbon oils such as olefin oligomers (PAOs),dibasic acid esters, polyol esters, and dewaxed waxy raffinate.Synthetic hydrocarbon base oils sold by the Shell Group under thedesignation “XHVI” (trade mark) may be conveniently used.

Effects of the Invention

(1) Novel phosphorus-free Mo-based friction-modifiers have beenobtained.

(2) The compounds of this invention exhibit a low friction coefficientand they can be used in particular as friction modifiers for varioustypes of energy-saving engine lubricating oils.

(3) The compounds of this invention are especially suitable for use asfriction-modifiers for fuel-saving engine oils as they arephosphorus-free.

(4) There is no damage to the catalysts (removal of NOx) which arehoused in automobile exhaust gas cleaning apparatus.

EXAMPLES

The invention is described below by means of Examples and ComparativeExamples but the invention is not limited in any way by these examples.

Example 1

The synthesis of Compound 6 in the aforementioned Table 1, the casewhere X is S, there is no Y and R¹ to R¹⁰ are CH₃.

(i) First Process

Tetrahydrofuran (THF, 45 ml) was added to 3.75 g (18.8 mmol) ofpentamethylcyclopentadiene and, after being cooled to −78° C., 12.5 ml(18.8 mmol) of Bu-Li were added dropwise and lithiumpentamethylcyclopentadienyl was co-ordinated. Then 5 g (18.8 mmol) ofmolybdenum hexa-carbonyl were added to this material and heated underreflux for 48 hours and, after the reaction had been completed, themother liquor was cooled to 0° C. Separately, 3.2 g (18.8 mmol) ofiron(II) sulphate was added to a solution comprising a mixture of 100 mlof pure water and 20 ml of acetic acid and the solution so obtained wasadded dropwise to the mother liquor. The red coloured solution obtainedwas subjected to suction filtration, washed and dried and thedi(pentamethylcyclopentadienyl)molybdenum hexa-carbonyl complex wasobtained by recrystallization. Yield 24%

(ii) Second Process

The di(pentamethylcyclopentadienyl)molybdenum hexa-carbonyl complex (0.5g, 0.79 mmol) and 0.69 g (5.84 mmol) of 3-sulphorane were dissolved in100 ml of toluene and heated under reflux at 120° C. for 3 hours. Afterthe reaction had been completed the solvent was removed and the reactionproduct was subjected to column chromatography and a red colouredcomplex was isolated. Yield 3%

Example 2

The synthesis of Compound 5 in the aforementioned Table 1, the casewhere X is S, Y is O and R¹ to R¹⁰ are CH₃.

The aforementioned di(heptamethylcyclopentadienyl)molybdenumhexa-carbonyl complex (0.5 g, 0.79 mmol) and 0.69 g (5.84 mmol) of3-sulphorane were dissolved in 100 ml of toluene and heated under refluxat 120° C. for 3 hours. After the reaction had been completed thesolvent was removed and the reaction product was subjected to columnchromatography and an orange coloured complex was isolated. Yield 4%

Example 3

The synthesis of Compound 3 in the aforementioned Table 1, the casewhere X and Y are O and R¹ to R¹⁰ are H.

(i) First Process

Tetrahydrofuran (THF, 45 ml) was added to 18.8 mmol of cyclopentadieneand, after being cooled to −78° C., 12.5 ml (18.8 mmol) of Bu-Li wereadded dropwise and the lithium pentamethylcyclopentadienyl wasco-ordinated. Then 5 g (18.8 mmol) of molybdenum hexa-carbonyl wereadded to this material and heated under reflux for 48 hours and, afterthe reaction had been completed, the mother liquor was cooled to 0° C.Separately, 3.2 g (18.8 mmol) of iron(II) sulphate was added to asolution comprising a mixture of 100 ml of pure water and 20 ml ofacetic acid and the solution so obtained was added dropwise to themother liquor. The red coloured solution obtained was subjected tosuction filtration, washed and dried and thedi(cyclo-pentadienyl)molybdenum hexa-carbonyl complex was obtained byrecrystallization. Yield 20%

(ii) Second Process

The di(cyclopentadienyl)molybdenum hexa-carbonyl complex (0.5 g, 1.02mmol) and 0.6 g (5.08 mmol) of 3-sulphorane were dissolved in 50 ml oftoluene and heated under reflux at 120° C. for 3 hours. After removingthe solvent the yellow coloured product di(cyclopentadienyl)μ-oxodioxomolybdenum complex was produced and isolated from the reactionmixture by means of column chromatography. Yield 34%

Example 4

The synthesis of Compound I in the aforementioned Table 1, the casewhere X is S, Y is O and R¹ to R¹⁰ are H.

Reaction in the same way as in Example 3 and the red coloured productdi(cyclopentadienyl) μ-thioxodioxomolybdenum complex was isolated bymeans of column chromatography. Yield 14%

Example 5

The complex obtained in Example 2 was adjusted in such a way as toprovide an Mo content of 500 ppm in engine oil (di-isononyl adipic acid)(viscosity at 100° C.: 3.04 mm²/s) to which 5% of a dispersing agent(alkenylsuccinic acid polyalkylene polyimide, trade name Infineum C9266)had been added.

Comparative Example 1

The case where the complex obtained in Example 2 had not been used inthe composition of Example 5 was taken as Comparative Example 1. Both ofthe compositions are shown in Table 20 below.

These sample oils were subjected to 30 minute friction coefficientmeasurement and evaluation under the conditions shown in Table 19 belowusing an SRV tester (a reciprocating movement tester of thecylinder-on-disc type shown in FIG. 2) and the results are shown inFIG. 1. The test piece was 52100 steel.

Testing Conditions

TABLE 19 Condition Parameter Load 400N Frequency 50 Hz Amplitude 1.5 mmTemperature 100° C. Sample Size 0.5 mm³

TABLE 20 Comparative Example 1 Example 5 Base Oil Ester oil (di-isononylEster oil (di- adipic acid) isononyl adipic acid) Friction-modifier Notadded Complex obtained in Example 2 Mo Content in the Oil ppm 0 500Alkenylsuccinic acid 5  5 polyalkylene polyimide (%)

The case of the Example 5 exhibited a low friction coefficient whencompared with the base oil with no addition (Comparative Example 1) from1 minute after the start of the test and it is clear that the compoundhad the function of a friction-modifier. That is to say, the compoundingof a friction-modifier of this invention clearly shows a lower frictioncoefficient when compared with the case where it has not beencompounded.

What is claimed is:
 1. The dicyclopentadienyl molybdenum crosslinked complex having general formula (2) below:

wherein R¹ to R¹⁰ are groups selected individually from the group comprising hydrogen, a methyl group and an ethyl group.
 2. The dicyclopentadienyl molybdenum crosslinked complex having general formula (4) below:

R¹ to R¹⁰ are groups selected individually from the group comprising hydrogen, a methyl group and an ethyl group. 